Relative Tumor Density of Soft-Tissue Sarcoma in Korean Population: An Institutional Review

被引:0
|
作者
Cha, Bo Bin [1 ]
Kim, Jung Yup [1 ]
Kim, Won-Serk [1 ]
Lee, Ga-Young [1 ]
Choi, Young-Jun [1 ]
机构
[1] Sungkyunkwan Univ, Kangbuk Samsung Hosp, Sch Med, Dept Dermatol, 29 Saemunan Ro, Seoul 03181, South Korea
关键词
DERMATOFIBROSARCOMA PROTUBERANS; KAPOSIS-SARCOMA; SQUAMOUS-CELL; HEAD; CLASSIFICATION; ANGIOSARCOMA; NECK; AGE;
D O I
10.5021/ad.23.122
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Comprehensive studies on the tumor burden of soft-tissue sarcoma (STS) by anatomical site are lacking in Asian populations. Objective: To investigate the anatomical distribution of STS via relative tumor density (RTD) in a Korean cohort. Methods: The RTDs of patients with STS at a single-institution from 2007-2022 were retrospectively analyzed. To describe the STS locations, the body was divided into 4 anatomical sites, and the RTD of each was calculated to the compare topographic tumor burden. Results: Fifty-nine cases in 58 individuals, 35 male (60.3%) and 23 female (39.7%), with a mean age of 56.5 +/- 20.4 were analyzed. Overall, the most frequent STS site was the lower extremity (LE, n=22, 37.3%), and the highest RTD was in the head and neck (H&N, 2.44; 95% confidence interval, 1.39-3.77). Dermatofibrosarcoma protuberans (DFSP), Kaposi's sarcoma (KS), and angiosarcoma (AS) accounted for 76.3% of all the cases. DFSP, KS, and AS showed significantly higher RTD on the trunk (2.55, p=0.025), LE (3.88, p<0.001), and H&N (7.42, p<0.001), respectively, than elsewhere. Conclusion: Each STS displays topographic variability and produces different topographic tumor burdens by body site in an Asian population.
引用
收藏
页码:96 / 104
页数:9
相关论文
共 50 条
  • [1] SOFT-TISSUE SARCOMA
    CACHAZA, JA
    RAVASSA, FO
    AVILA, IR
    DEABAJO, MB
    MEDICINA CLINICA, 1991, 97 (10): : 396 - 396
  • [2] Soft-tissue Sarcoma
    Gilbert, Nathan E.
    Cannon, Christopher P.
    Lin, Patrick P.
    Lewis, Valerae O.
    JOURNAL OF THE AMERICAN ACADEMY OF ORTHOPAEDIC SURGEONS, 2009, 17 (01) : 40 - 47
  • [3] SOFT-TISSUE SARCOMA
    BASELGA, J
    MEDICINA CLINICA, 1991, 96 (01): : 16 - 17
  • [4] SOFT-TISSUE SARCOMA
    GANGULY, PK
    SCOTTISH MEDICAL JOURNAL, 1975, 20 (05) : 272 - 273
  • [5] SOFT-TISSUE SARCOMA
    FUCHS, R
    DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1986, 111 (35) : 1342 - 1342
  • [6] SARCOMA OF SOFT-TISSUE
    SUIT, HD
    CA-A CANCER JOURNAL FOR CLINICIANS, 1978, 28 (05) : 284 - 295
  • [7] SOFT-TISSUE SARCOMA
    VINEIS, P
    SARACCI, R
    KOGEVINAS, M
    BOFFETTA, P
    CANCER CAUSES & CONTROL, 1992, 3 (05) : 493 - 494
  • [8] SOFT-TISSUE SARCOMA IN KUWAIT - A REVIEW OF 114 PATIENTS
    AHMED, MJ
    OMAR, YT
    ALI, SM
    TEMMIM, L
    CLINICAL RADIOLOGY, 1987, 38 (01) : 27 - 29
  • [9] PROGNOSIS IN SOFT-TISSUE SARCOMA
    ROOSER, B
    ACTA ORTHOPAEDICA SCANDINAVICA, 1987, 58 : 5 - 52
  • [10] RADIOTHERAPY OF SOFT-TISSUE SARCOMA
    HOLFELD, H
    SCHERER, E
    CHIRURG, 1977, 48 (11): : 696 - 700